2015
DOI: 10.5966/sctm.2015-0006
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Study of Bone Marrow and Embryonic Stem Cell-Derived Human Mesenchymal Stem Cells for Treatment ofEscherichia coliEndotoxin-Induced Acute Lung Injury in Mice

Abstract: To determine the optimal source of mesenchymal stem cells (MSCs) for cell-based therapy for acute lung injury, bone marrow (BM)- and embryonic stem cell-derived human MSC (ES-MSCs) were compared as therapeutic agents for Escherichia coli endotoxin-induced lung injury in mice. ES-MSCs behaved similarly to BM-MSCs by markedly decreasing the inflammatory response induced by endotoxin. However, unlike BM-MSCs, ES-MSCs provided no protective effects against increasing lung water and protein permeability, in part be… Show more

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Cited by 64 publications
(57 citation statements)
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“…Exosomes (microvesicles) secreted from MSCs may play a pivotal bi-directional role in communication between stem cell and injured cell. Consequently, the stem cell phenotype can be induced to facilitate self-repair or to acquire specific features of the tissue [Hao et al, 2015]. Such microvesicles derived from BM-MSCs have been shown to exert a protective role in acute pancreatitis induced by sodium taurocholate [Yin et al, 2016] and preserve insulin-producing cells in the islets of mice with type I DM [Shigemoto-Kuroda et al, 2017].…”
Section: Discussionmentioning
confidence: 99%
“…Exosomes (microvesicles) secreted from MSCs may play a pivotal bi-directional role in communication between stem cell and injured cell. Consequently, the stem cell phenotype can be induced to facilitate self-repair or to acquire specific features of the tissue [Hao et al, 2015]. Such microvesicles derived from BM-MSCs have been shown to exert a protective role in acute pancreatitis induced by sodium taurocholate [Yin et al, 2016] and preserve insulin-producing cells in the islets of mice with type I DM [Shigemoto-Kuroda et al, 2017].…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, hESC-derived MSCs performed more effectively compared to bone marrow MSCs in reducing experimental autoimmune encephalitis [97], pulmonary hypertension [98], and acute pulmonary injury [99], and hiPSC-derived MSCs outperformed bone marrow MSCs in a mouse model of anthracycline-induced cardiomyopathy [100]. MB-derived MSCs have already been tested mouse models of hindlimb ischemia and chronic airway disease.…”
Section: Mb Potential For Cellular Therapiesmentioning
confidence: 99%
“…Administration of BM‐MSCs significantly reduced the influx of white blood cells, neutrophils and decreasing the secretion of the inflammatory cytokines, macrophage inflammatory protein‐2, and tumor necrosis factor‐α, in the injured alveolus. BM‐MSCs also reduced extravascular lung water and the total protein levels …”
Section: Discussionmentioning
confidence: 99%